Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C233/00—Carboxylic acid amides
  • C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
  • C07C233/45—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups
  • C07C233/46—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom
  • C07C233/47—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom having the carbon atom of the carboxamide group bound to a hydrogen atom or to a carbon atom of an acyclic saturated carbon skeleton
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P25/00—Drugs for disorders of the nervous system
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P25/00—Drugs for disorders of the nervous system
  • A61P25/08—Antiepileptics; Anticonvulsants
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P25/00—Drugs for disorders of the nervous system
  • A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P25/00—Drugs for disorders of the nervous system
  • A61P25/24—Antidepressants
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P25/00—Drugs for disorders of the nervous system
  • A61P25/26—Psychostimulants, e.g. nicotine, cocaine
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P25/00—Drugs for disorders of the nervous system
  • A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia

Definitions

• This invention relates to 2-pentanoylaminoacetic acid (I) and to pharmaceutical acceptable metal salts and addition salts with bases derived thereof, for use as pharmaceuticals.
• the metal salts may be, for example, a sodium, a potassium, a lithium, a calcium, a magnesium, an aluminium or an iron salt.
• the addition salts may be formed by reaction with an inorganic base such as ammonia, or with an organic base which may be an aliphatic, a cycloaliphatic or an heterocyclic base, such as, for example, ethylamine, diethylamine, triethylamine, isopropylamine, ethanolamine, diethanolamine, triethanolamine.
• Said organic base may also be an amino-acid natural or not, such as, for example, lysine, ornithine or arginine.
• a preferred salt of 2-pentanoylaminoacetic acid is the sodium salt.
• the compound of the present invention 2-pentanoylaminoacetic acid, is known for several years.
• compositions comprising compound I or a pharmaceutically acceptable salt thereof present great interest for producing an effect on the central nervous system, in particular in the treatment of various forms of epilepsy, in the treatment of dyskinesiae such as, for example, parkinsonism, in the treatment of memory troubles, of psychic troubles such as, for example, depression, and in the treatment of cerebral anoxia.
• the compounds tested have been administered orally to 20 mice (CDl-Charles River) at a dose of 10 mg/kg as a suspension in a 1% tragacanth gum mucilage. Administration has been done by means of an intragastric tube.
• bicuculline has been administered at a dose of 0,7 mg/kg by intravenous injection in the lateral vein of the tail.
• the anti-convulsant activity of the compounds has been further evaluated, using the technique described hereinabove, by examining the effect at different doses. From the experimental data, the ED 50 value has been calculated, i.e. the effective dose (mg/kg) providing protection against tonic extension of 50% of the animals. The results obtained are the following:
• the drug to be tested has been administered orally as a 1% tragacanth gum mucilage, by means of an intragastric tube to groups of 3 or 5 mice, fasted for 18 hours.
• the compounds have been tested at a dose decreasing in a logarithmic way, starting from 3000 mg/kg, i.e. 3000, 1000, 300, 100, 30 and 10 mg/kg. No further testing has been made when a dose has been reached at which no abnormal behaviour or toxicity has been observed.
• Behaviour has been studied 2, 4, 6 and 24 hours after treatment and the observation has been extended if symptoms persisted at that moment. The deaths were registered for 14 days following the treatment.
• the LD 50 value i.e. the dose expressed in mg/kg which is lethal for 50% of the animals, has been calculated according to the Litchfield and Wilcoxon method [J. Pharmacol. Exp. Ther., 96, 99 (1949)].
• 2-pentanoylaminoacetic acid and its sodium salt are better than sodium valproate; their superiority is evidenced quantitatively by means of the therapeutical indexes TI-A and TI-B which corresponds, respectively, to the ratio of the LD 50 /ED 50 values and to the ratio of the MTD/ED 50 values.
• the values of these therapeutical indexes are the following:
• A is such that the radical --CO--A represents, for example, a carboxylic group, an alkoxycarbonyl group, an acide halide group, an anhydride group, a carbamoyl group or a N-carbonylimidazole group.
• Y represents: either the CH 2 --COOH group, either a precursor of said CH 2 --COOH group, such as:
• Z represents, for example, an alkoxycarbonyl group or a formyl group optionally used in a protected form such as, e.g. a dithioacetal group, which may be cyclic or not.
• B 1 and B 2 which can be identical or not, represent, for example, an alkoxycarbonyl group on a carboxylic group.
• the acylation of amine IV by reagent III can directly yield compound I or a salt thereof, or yield intermediate V, which optionally can be isolated or not, before it is converted into compound I or a salt thereof.
• the acylation is usually carried out by reacting compound III with at least two equivalents of amine IV, or with one equivalent of amine IV and at least one equivalent of an organic or inorganic base, such as, for example, a tertiary amine, pyridine, an hydroxyde or a carbonate of an alkali or earthalkali metal.
• an organic or inorganic base such as, for example, a tertiary amine, pyridine, an hydroxyde or a carbonate of an alkali or earthalkali metal.
• the reaction is carried out in an inert solvent or an excess of the organic base is used as solvent.
• the acylation of compound IV is classically made in the presence of a dehydrating agent such as, for example, phosphorus pentoxyde, or of a coupling agent such as, for example, dicyclohexylcarbodiimide or 1,1'-carbonylidiimidazole.
• a dehydrating agent such as, for example, phosphorus pentoxyde
• a coupling agent such as, for example, dicyclohexylcarbodiimide or 1,1'-carbonylidiimidazole.
• Y in the intermediate V, represents a precursor of the --CH 2 --COOH group, it is converted into said carboxymethyl group by well-known methods, chosen according to the nature of the group Y, such as, for example:
• hydrolysis carried out in an aqueous or alcoholic-aqueous medium in the presence of an acidic or basic catalyst,
• 2-pentanoylaminoacetic acid is obtained in the form of a metal or an addition salt, it can be transformed into the free carboxylic form by treatment with a suitable acid. Conversion of one salt into another salt can also be made by art-known methods.
• compositions may be formulated in order to be administered orally, rectally or parenterally, containing at least an effective amount of said compound or a salt thereof, usually in the presence of at least one pharmaceutical excipient.
• the compositions to be administered orally can be liquids or solids and exist as tablets, sugar-coated pills, coated tablets, capsules, granules, powders, syrups or suspensions.
• the dry oral formulations comprise additives and excipients commonly used in galenic pharmacy, inert diluents, disintegration agents, binders and lubricants, such as lactose, starch, talc, gelatin, stearic acid, cellulose and derivatives thereof, silicilic acid, magnesium stearate, polyvinylpyrrolidone, calcium phosphate, calcium carbonate and the like.
• Such preparations can be made in order to prolong disintegration and consequently the active duration of the active element.
• aqueous suspensions, the emulsions and the oily solutions are prepared in the presence of sweetening agents, such as dextrose or glycerol, flavouring agents, such as vanillin for example, and can also contain thickening agents, wetting agents and preservation agents.
• sweetening agents such as dextrose or glycerol
• flavouring agents such as vanillin for example
• the oily emulsions and solutions are prepared in an oil of vegetal or animal origin and can contain emulsifiers, flavouring, dispersing, sweetening and antioxidant agents.
• emulsifiers for parenteral administration, sterile water, an aqueous polyvinylpyrrolidone solution, peanut oil ethyl oleate and the like are used as a vehicle.
• aqueous or oily injectable solutions can contain thickening, wetting, dispersing and gelling agents.
• compositions to be administered rectally may be solids or liquids and may be presented in the form of suppositories, of gels, of solutions, of emulsions or of suspensions.
• the suppositories may be prepared using fats such as cacao butter or semi-synthetic substances derived from triglycerids, or using hydrosoluble products such as mixtures or polyethyleneglycols.
• the daily dose for administration of compound I or a salt thereof will be 100 mg to 5 g.
• the aforementioned pharmaceutical compositions are usually formulated in dosage unit form, the unit dose being 100 mg to 1 g.
• the daily dose may be increased without danger, due to the low toxicity of compound I and its pharmaceutical suitable salts.
• the active product is designated by "compound A”, which is either 2-pentanoylaminoacetic acid either sodium 2-pentanoylaminoacetate.

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• Health & Medical Sciences (AREA)
• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Engineering & Computer Science (AREA)
• Bioinformatics & Cheminformatics (AREA)
• Biomedical Technology (AREA)
• Neurology (AREA)
• Neurosurgery (AREA)
• General Chemical & Material Sciences (AREA)
• Life Sciences & Earth Sciences (AREA)
• Veterinary Medicine (AREA)
• Medicinal Chemistry (AREA)
• Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
• Public Health (AREA)
• Pharmacology & Pharmacy (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Animal Behavior & Ethology (AREA)
• General Health & Medical Sciences (AREA)
• Psychiatry (AREA)
• Pain & Pain Management (AREA)
• Hospice & Palliative Care (AREA)
• Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
• Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

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Citations (5)

• 1983
  • 1983-06-30 LU LU84891A patent/LU84891A1/fr unknown
• 1984
  • 1984-06-21 DE DE8484200904T patent/DE3474912D1/de not_active Expired
  • 1984-06-21 EP EP84200904A patent/EP0130644B1/en not_active Expired
  • 1984-06-25 US US06/624,110 patent/US4562205A/en not_active Expired - Lifetime
  • 1984-06-26 IL IL72227A patent/IL72227A/xx unknown
  • 1984-06-26 AU AU29896/84A patent/AU563134B2/en not_active Ceased
  • 1984-06-28 JP JP59132122A patent/JPS6036412A/ja active Granted
  • 1984-06-29 ZA ZA844971A patent/ZA844971B/xx unknown
  • 1984-06-29 DK DK323284A patent/DK323284A/da not_active Application Discontinuation

Patent Citations (6)

Non-Patent Citations (16)

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